Vitamin D deficiency and VDR TaqI polymorphism on diabetic nephropathy risk among type 2 diabetes patients.

IF 3.9 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Frontiers in Endocrinology Pub Date : 2025-06-12 eCollection Date: 2025-01-01 DOI:10.3389/fendo.2025.1567716
Addisu Melake, Misganaw Asmamaw Mengstie
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引用次数: 0

Abstract

Background: Many studies have shown that vitamin D deficiency and vitamin D receptor TaqI gene polymorphisms are associated with susceptibility to diabetic nephropathy in various populations. The objective of this study was to determine the impact of vitamin D deficiency and vitamin D receptor TaqI gene polymorphism on the risk of diabetic nephropathy complications in T2DM at the Debre Tabor Comprehensive Specialized Hospital, Northwest Ethiopia.

Methods: A total of 210 participants, including 70 diabetic patients with nephropathy, 70 diabetic patients without nephropathy, and 70 healthy controls, participated in an age-and sex-matched hospital-based case-control study. Demographic and clinical data were assessed to determine the related risk factors. DNA was extracted from blood samples and subjected to polymerase chain reaction and agarose gel electrophoresis analysis to determine the TaqI genotypes.

Results: Vitamin D deficiency was detected in our investigation, and it was much more prevalent in diabetic nephropathy patients than type 2 diabetic patients and controls (OR = 5.05, 95% CL = 2.03-12.53; P < 0.001). Moreover, both the TaqI tt genotype (OR: 2.48; 95% CL: 1.15-5.37; P=0.020) and t allele (OR: 1.70; 95% CL: 1.13-2.57; P=0.010) were substantially more prevalent in diabetic nephropathy patients than in type 2 diabetic patients and controls, indicating that it may be a major risk factor for the development of diabetic nephropathy.

Conclusions: The findings point to a potential link between vitamin D deficiency and diabetic nephropathy complications. Moreover, TaqI gene polymorphisms have been linked to an increased risk of developing the disease in the Ethiopian population under study.

维生素D缺乏和VDR TaqI多态性与2型糖尿病患者糖尿病肾病风险的关系
背景:许多研究表明,维生素D缺乏和维生素D受体TaqI基因多态性与不同人群的糖尿病肾病易感性有关。本研究的目的是确定维生素D缺乏和维生素D受体TaqI基因多态性对埃塞俄比亚西北部Debre Tabor综合专科医院T2DM患者糖尿病肾病并发症风险的影响。方法:共有210名参与者,包括70名合并肾病的糖尿病患者,70名无肾病的糖尿病患者和70名健康对照者,参加了一项年龄和性别匹配的基于医院的病例对照研究。对人口统计学和临床资料进行评估,以确定相关的危险因素。从血样中提取DNA,进行聚合酶链反应和琼脂糖凝胶电泳分析,确定TaqI基因型。结果:糖尿病肾病患者存在维生素D缺乏症,其发生率明显高于2型糖尿病患者和对照组(OR = 5.05, 95% CL = 2.03-12.53;P 0.001)。此外,TaqI tt基因型(OR: 2.48;95% cl: 1.15-5.37;P=0.020)和t等位基因(OR: 1.70;95% cl: 1.13-2.57;P=0.010)在糖尿病肾病患者中明显高于2型糖尿病患者和对照组,提示它可能是糖尿病肾病发生的主要危险因素。结论:研究结果指出维生素D缺乏与糖尿病肾病并发症之间存在潜在联系。此外,TaqI基因多态性与研究中的埃塞俄比亚人口患病风险增加有关。
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来源期刊
Frontiers in Endocrinology
Frontiers in Endocrinology Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
5.70
自引率
9.60%
发文量
3023
审稿时长
14 weeks
期刊介绍: Frontiers in Endocrinology is a field journal of the "Frontiers in" journal series. In today’s world, endocrinology is becoming increasingly important as it underlies many of the challenges societies face - from obesity and diabetes to reproduction, population control and aging. Endocrinology covers a broad field from basic molecular and cellular communication through to clinical care and some of the most crucial public health issues. The journal, thus, welcomes outstanding contributions in any domain of endocrinology. Frontiers in Endocrinology publishes articles on the most outstanding discoveries across a wide research spectrum of Endocrinology. The mission of Frontiers in Endocrinology is to bring all relevant Endocrinology areas together on a single platform.
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